| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42128216G>T | CA10264875 | CYP2D6 | c.648C>A (p.Pro216=) c.801C>A (p.Pro267=) c.468C>A (p.Pro156=) c.735C>A (p.Pro245=) n.1525C>A c.657C>A (p.Pro219=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42128216G>A | CA514800281 | CYP2D6 | c.648C>T (p.Pro216=) c.801C>T (p.Pro267=) c.468C>T (p.Pro156=) c.735C>T (p.Pro245=) n.1525C>T c.657C>T (p.Pro219=) | dbSNP |
| 22 | g.42128216G= | CA2406579015 | CYP2D6 | c.648C= (p.Pro216=) c.801C= (p.Pro267=) c.468C= (p.Pro156=) c.735C= (p.Pro245=) n.1525C= c.657C= (p.Pro219=) | dbSNP |